Down-regulation of intestinal scavenger receptor class B, type I (SR-BI) expression in rodents under conditions of deficient bile delivery to the intestine

PJ Voshol, M Schwarz, A Rigotti, M Krieger, AK Groen, F Kuipers*

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    60 Citations (Scopus)

    Abstract

    Scavenger receptor class B, type I (SR-BI) is expressed in the intestines of rodents and has been suggested to be involved in the absorption of dietary cholesterol. The aim of this study was to determine whether intestinal SR-BI expression is affected in animal models with altered bile delivery to the intestine and impaired cholesterol absorption. SR-BI protein and mRNA levels were determined in proximal and distal small intestine from control, bile-duct-ligated and bile-diverted rats and from control and bile-duct-ligated mice. Two genetically altered mouse models were studied: multidrug resistance-2 P-glycoprotein-deficient [Mdr2((-/-))] mice that produce phospholipid/cholesterol-free bile, and cholesterol 7 alpha -hydroxylase-deficient [Cyp7a((-/-))] mice, which exhibit qualitative and quantitative changes in the bile-salt pool. Cholesterol-absorption efficiency was quantified using a dual-isotope ratio method. SR-BI was present at the apical membrane of enterocytes in control rats and mice and was more abundant in proximal than in distal segments of the intestine. In bile-duct-ligated animals, levels of SR-BI protein were virtually absent and mRNA levels were decreased by approximate to 50 %. Bile-diverted rats, Mdr2((-/-)) mice and Cyp7a((-/-)) mice showed decreased levels of intestinal SR-BI protein while mRNA levels were unaffected. Cholesterol absorption was reduced by > 90% in bile-duct-ligated and bile-diverted animals and in Cyp7a((-/-)) mice, whereas Mdr2((-/-)) mice showed an approximate to 50% reduction. This study shows that SR-BI is expressed at the apical membrane of enterocytes of rats and mice; mainly in the upper intestine where cholesterol absorption is greatest, and indicates that bile components play a role in post-transcriptional regulation of SR-BI expression. Factors associated with cholestasis appear to be involved in transcriptional control of intestinal SR-BI expression. The role of SR-BI in the cholesterol-absorption process remains to be defined.

    Original languageEnglish
    Pages (from-to)317-325
    Number of pages9
    JournalBiochemical Journal
    Volume356
    Publication statusPublished - 1-Jun-2001

    Keywords

    • absorption
    • bile salts
    • cholesterol
    • knockout mouse
    • phospholipid
    • DENSITY-LIPOPROTEIN RECEPTOR
    • CHOLESTEROL 7-ALPHA-HYDROXYLASE GENE
    • PHYSICAL-CHEMICAL BEHAVIOR
    • PLASMA RATIO METHOD
    • ADULT HUMAN-BEINGS
    • DIETARY-CHOLESTEROL
    • BILIARY CHOLESTEROL
    • AGGREGATION STATES
    • LINOLEIC-ACID
    • HDL RECEPTOR

    Fingerprint

    Dive into the research topics of 'Down-regulation of intestinal scavenger receptor class B, type I (SR-BI) expression in rodents under conditions of deficient bile delivery to the intestine'. Together they form a unique fingerprint.

    Cite this